sick with this embarassing disease
it is really frustrating to be socially isolated because your sweat glands keep on reproducing huge amount of sweat without even having the tiniest bit of control to stop it. it is also depressing that you're 18 but haven't been on a relationship yet, even if you have a pretty face and a good personality.
oh my social life has long been on the bottom. i refuses romantic dates, skip fun in hanging out with my friends, almost thought of dropping off to school and make my life more miserable by staying my whole life on my own room. i can't even put my arms on my best friend's shoulder cause I'm afraid she might freak out or what.
i shy out when i begin to feel a sweat breaking off on my skin. it is because I'm afraid the next thing that's going to happen is the faucet-like-pores on my armpits will begin to burst it content in no time. and what should i do afterwards? i would be on the corner, looking paranoid with my arms glued to my side.
I've always been on the campus rumor and i keep overhearing others talking about the abnormality of my pores that i sweat more than their bodies can sweat. most people are cruel, and they don't even give me a break. I'm a very talented person, i can sing, i can draw, and there's a whole lot of thing i can show them that I'm better off than people who's life is well dedicated in picking up on people and calling them names.
In my chosen profession which is nursing, I often got ask by my patients if I am nervous or if it's my first time because I often leave sweat stain in my BP cuff whenever i obtain their blood pressure, and i remember the most horrible reaction i got is when I've put a simple IV catheter into a man's vein and i slip that thing and pushed it to a wrong vein so i was preparing to reinsert it but the patient refuses and ask for another nurse to perform the reinsertion. and the only culprit was my sweaty palm.
i've thought that i'm sick, that there is no cure to this. but now i've learned that there's a whole lot of sweaty duds out there who has the same problem, i am lucky i found this site in the internet today and i am getting ready to befriend other people with HH.
you guys, i can relate with each of you who sweats to death. i only tried one thing since the last 12 years of suffering from this disease and that is the thing i bought in the pharmacy just last month.
it is the topical antiperspirant available in the pharmacy without prescription. as of experience, this thing works for me and i could recommend Driclor to the rest.
ok hear this, you should be careful with this though, the side effects may be the cause of concern, before application you should read the instructions in the box and follow it very carefully. because if you applied it wrongly, you'll gonna end up scratching badly your armpits and woke up in the morning with sore underarms. believe me, that was based from personal experience.
so best of luck to everyone..
if you ever need an advice you can message me, and i can help you as i can..
oh my social life has long been on the bottom. i refuses romantic dates, skip fun in hanging out with my friends, almost thought of dropping off to school and make my life more miserable by staying my whole life on my own room. i can't even put my arms on my best friend's shoulder cause I'm afraid she might freak out or what.
i shy out when i begin to feel a sweat breaking off on my skin. it is because I'm afraid the next thing that's going to happen is the faucet-like-pores on my armpits will begin to burst it content in no time. and what should i do afterwards? i would be on the corner, looking paranoid with my arms glued to my side.
I've always been on the campus rumor and i keep overhearing others talking about the abnormality of my pores that i sweat more than their bodies can sweat. most people are cruel, and they don't even give me a break. I'm a very talented person, i can sing, i can draw, and there's a whole lot of thing i can show them that I'm better off than people who's life is well dedicated in picking up on people and calling them names.
In my chosen profession which is nursing, I often got ask by my patients if I am nervous or if it's my first time because I often leave sweat stain in my BP cuff whenever i obtain their blood pressure, and i remember the most horrible reaction i got is when I've put a simple IV catheter into a man's vein and i slip that thing and pushed it to a wrong vein so i was preparing to reinsert it but the patient refuses and ask for another nurse to perform the reinsertion. and the only culprit was my sweaty palm.
i've thought that i'm sick, that there is no cure to this. but now i've learned that there's a whole lot of sweaty duds out there who has the same problem, i am lucky i found this site in the internet today and i am getting ready to befriend other people with HH.
you guys, i can relate with each of you who sweats to death. i only tried one thing since the last 12 years of suffering from this disease and that is the thing i bought in the pharmacy just last month.
it is the topical antiperspirant available in the pharmacy without prescription. as of experience, this thing works for me and i could recommend Driclor to the rest.
ok hear this, you should be careful with this though, the side effects may be the cause of concern, before application you should read the instructions in the box and follow it very carefully. because if you applied it wrongly, you'll gonna end up scratching badly your armpits and woke up in the morning with sore underarms. believe me, that was based from personal experience.
so best of luck to everyone..
if you ever need an advice you can message me, and i can help you as i can..
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